Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Arrest of bone development AND/OR growth |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Trochlear notch incongruity (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital anomaly of skeletal bone |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Radial aplasia-thrombocytopenia syndrome |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Craniotabes |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ununited anconeal process |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Canine hypertrophic osteodystrophy |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Juvenile osteochondrosis of upper extremity (disorder) |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Juvenile osteochondrosis of lower extremity |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Juvenile osteochondrosis of lower ulna |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Developmental anomaly of odontoid process of axis (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Os acromiale (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Persistent human tail |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital metatarsus valgus |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Median palatal cyst (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Metatarsus adductus |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies). |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital laryngomalacia (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Iniencephaly |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital thickening of talus |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Failure of differentiation of bones of forearm (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Talipes (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
anomalie transverse du bras au niveau de l'avant-bras |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital prognathism |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Myelocele |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Rudimentary patella |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital macrognathism |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Genu recurvatum and long leg bone bowing (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Bifid patella |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital enlargement of fontanel |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cleft lip and cleft of alveolar process of maxilla (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hajdu-Cheney syndrome |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital thickening of tarsal bone |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Supernumerary tarsal bone |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Oto-onycho-peroneal syndrome (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital perforation of the nasal sinus wall |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital leg bone bowing (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ecchordosis physaliphora (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Plantarflexed cuboid |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Duplication of lower limb bone |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital hip dysplasia (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transverse arrest carpal level |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital bony fusion of phalanges (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital spinal meningocele |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Failure of differentiation of bones of lower limb |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Chondroectodermal dysplasia (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ectromelia |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Spinal meningocele |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital cerebral meningocele |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hydrencephalomeningocele |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Brachymetapody |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital failure of fusion between maxillary and mandibular processes (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cleft of alveolar ridge (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Spondyloschisis |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital malposition of nasal turbinate |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Spina bifida |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Defect of vertebral segmentation |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Brachyrachia (short spine dysplasia) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Metatarsus varus |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Lumbosacral prespondylolisthesis |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Lateral developmental cyst of jaw |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Platyspondylia |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital malposition of metacarpal bone |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Duplication of radius |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Duplication of humerus |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital bent ulna (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital bent humerus |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoplasia of maxillary bone (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital bent radius (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoplasia of mandibular bone (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acquired hypoplasia of zygomatic bone |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Bilateral coronoid hypoplasia of mandible |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Bilateral condylar hypoplasia of mandible |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Condylar hypoplasia with mandibular asymmetry |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mandibular alveolar hypoplasia |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoplasia of radius (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fronto-parietal craniofaciosynostosis |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Interfrontal craniofaciosynostosis (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Parieto-occipital craniosynostosis |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
An ectopic tooth that has erupted on the lingual aspect of the maxilla or mandible. |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Buccal bifurcation cyst |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Calcaneonavicular bar (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoplasia of mandibular condyle |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fibrous cortical defect |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mandibular prognathism |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Maxillary prognathism |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mandibular retrognathism (disorder) |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Maxillary retrognathism |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Atelosteogenesis/diastrophic dysplasia |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Atelosteogenesis type 2 |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
An extremely rare genetic multisystemic disorder with characteristics of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anaemia, which may be accompanied by neutrophilic dermatosis. The disease can be associated with fever, joint pain, delayed bone age, growth failure, short adult stature, and development of flexion contractures. Other reported manifestations include failure to thrive, hepatomegaly, neutropenia, and transient cholestatic jaundice. The clinical course is chronic. Caused by a mutation in LPIN2 (18p11.31), which encodes phosphatidate phosphatase LPIN2 (Lipin-2), important in lipid metabolism. Follows an autosomal recessive pattern of inheritance. |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Partially impacted tooth in bone |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Completely impacted tooth in bone |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Segmental odontomaxillary dysplasia (disorder) |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fetal spina bifida (disorder) |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fetal sacral teratoma (disorder) |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Bone turnover rate disorder |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Juvenile idiopathic generalised osteoporosis |
Is a |
False |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hemimaxillofacial dysplasia (disorder) |
Is a |
True |
Disorder of bone development |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|